Evidence map›Paper›PMID 32738299›Full record

ArticleNanomedicine : nanotechnology, biology, and medicine2020

Liposomal formulation of HIF-1α inhibitor echinomycin eliminates established metastases of triple-negative breast cancer.

Christopher M Bailey, Yan Liu, Gong Peng, Huixia Zhang, Miao He, Duxin Sun, Pan Zheng, Yang Liu, Yin Wang

Open access · greenAbstract read
In one paragraph

Article in Nanomedicine : nanotechnology, biology, and medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
2.8field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

34 citing papers in PubMed, 45 citations in OpenAlex.

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  7. HIF-1 and HIF-2 in cancer: structure, regulation, and therapeutic prospects.Cellular and molecular life sciences : CMLS · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 3 countries.

Christopher M BaileyDivision of Immunotherapy, Institute of Human Virology, Department of Surgery and Comprehensive Cancer Center, University of Maryland School of Medicine, Baltimore, MD; Graduate Program in Molecular Medicine, The George Washington University School of Medicine and Health Sciences, Washington, D.C.
Yan LiuDivision of Immunotherapy, Institute of Human Virology, Department of Surgery and Comprehensive Cancer Center, University of Maryland School of Medicine, Baltimore, MD.
Gong PengInstitute of Translational Medicine, The First Hospital, Jilin University, Changchun, China.
Huixia ZhangDepartment of Pharmaceutical Sciences, University of Michigan, Ann Arbor, MI.
Miao HeDepartment of Pharmaceutical Sciences, University of Michigan, Ann Arbor, MI.
Duxin SunDepartment of Pharmaceutical Sciences, University of Michigan, Ann Arbor, MI.
Pan ZhengDivision of Immunotherapy, Institute of Human Virology, Department of Surgery and Comprehensive Cancer Center, University of Maryland School of Medicine, Baltimore, MD; Oncoimmune, Inc., Rockville, MD.
Yang LiuDivision of Immunotherapy, Institute of Human Virology, Department of Surgery and Comprehensive Cancer Center, University of Maryland School of Medicine, Baltimore, MD; Oncoimmune, Inc., Rockville, MD. Electronic address: yaliu@ihv.umaryland.edu.
Yin WangDivision of Immunotherapy, Institute of Human Virology, Department of Surgery and Comprehensive Cancer Center, University of Maryland School of Medicine, Baltimore, MD. Electronic address: yin.wang@ihv.umaryland.edu.
University of Maryland, Baltimore · USUniversity of Michigan · USJilin University · CN

Funding

Targeted Elimination of Cancer Stem Cells for AML TherapyR01CA171972 · NCI · CHILDREN'S RESEARCH INSTITUTE · PI LIU, YANG, MALEK, SAMI NIMER · 2013 to 2017
$2.3M
Therapeutic Elimination of Stem Cells for Relapsed Pediatric AMLU01CA183030 · NCI · CHILDREN'S RESEARCH INSTITUTE · PI LIU, YANG, SCHORE, REUVEN J · 2014 to 2017
$2.3M
Molecular Programs for Stem Cells of Hematological MalignanciesR21CA164469 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WANG, YIN · 2012 to 2013
$379k
CCR NIH HHS HHSN261200800001CNCI NIH HHS HHSN261200800001ENCI NIH HHS R01 CA171972NCI NIH HHS R21 CA164469NCI NIH HHS U01 CA183030
6 · The paper itself

Abstract

Hypoxia-inducible factor 1α (HIF-1α) is recognized as a prime molecular target for metastatic cancer. However, no specific HIF-1α inhibitor has been approved for clinical use. Here, we demonstrated that in vivo efficacy of echinomycin in solid tumors with HIF-1α overexpression is formulation-dependent. Compared to previously-used Cremophor-formulated echinomycin, which was toxic and ineffective in clinical trials, liposomal-echinomycin provides significantly more inhibition of primary tumor growth and only liposome-formulated echinomycin can eliminate established triple-negative breast cancer (TNBC) metastases, which are the leading cause of death from breast cancer, as available therapies remain minimally effective at this stage. Pharmacodynamic analyses reveal liposomal-echinomycin more potently inhibits HIF-1α transcriptional activity in primary and metastasized TNBC cells in vivo, the latter of which are HIF-1α enriched. The data suggest that nanoliposomal-echinomycin can provide safe and effective therapeutic HIF-1α inhibition and could represent the most potent HIF-1α inhibitor in prospective trials for metastatic cancer.

Indexed as

AnimalsCell Line, TumorEchinomycinFemaleHumansHypoxia-Inducible Factor 1, alpha SubunitLiposomesMiceNeoplasm MetastasisTriple Negative Breast NeoplasmsXenograft Model Antitumor AssaysEchinomycinHIF1A protein, humanHypoxia-Inducible Factor 1, alpha SubunitLiposomesBreast cancerEchinomycinHIF-1αLiposomeNanomedicine

Identifiers

PMID32738299
PMCPMC7508926
OpenAlexW3045578426

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.